Type 1 hyperlipoproteinemia in a child with large homozygous deletion encompassing GPIHBP1
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference32 articles.
1. Genetic bases of hypertriglyceridemic phenotypes;Johansen;Curr Opin Lipidol,2011
2. Genotype-phenotype relationships in patients with type I hyperlipoproteinemia;Chokshi;J Clin Lipidol,2014
3. Chylomicronaemia-current diagnosis and future therapies;Brahm;Nat Rev Endocrinol,2015
4. The acidic domain of GPIHBP1 is important for the binding of lipoprotein lipase and chylomicrons;Gin;J Biol Chem,2008
5. Glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 and the intravascular processing of triglyceride-rich lipoproteins;Adeyo;J Intern Med,2012
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1. Sequence Analysis of Six Candidate Genes in Miniature Schnauzers with Primary Hypertriglyceridemia;Genes;2024-01-31
2. The GPIHBP1-LPL complex and its role in plasma triglyceride metabolism: Insights into chylomicronemia;Biomedicine & Pharmacotherapy;2023-12
3. A homozygous variant in the GPIHBP1 gene in a child with severe hypertriglyceridemia and a systematic literature review;Frontiers in Genetics;2022-08-16
4. Primär genetische Dyslipoproteinämien und Atheroskleroserisiko;Pädiatrische Fettstoffwechselstörungen und Atheroskleroserisiko – kompakt;2022
5. Current Diagnosis and Management of Primary Chylomicronemia;Journal of Atherosclerosis and Thrombosis;2021-09-01
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